化工社化工社 化学情報印刷レポート · 研究参考用
Hydrochloric Acid → 3-(1-Hydroxy-2,2,2-trifluoro-1-trifluoromethylethyl)-2-methyl-7-nitrobenzo[b]furan
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | Hexafluoroacetone | HCID 12695 | — |
| 反応物 | Hexafluoroacetone trihydrate | HCID 36719 | — |
| 反応物 | Aluminum(III) Chloride | HCID 6451240 | — |
| 反応物 | 2-Methyl-7-nitrobenzofuran | HCID 13201897 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 3-(1-Hydroxy-2,2,2-trifluoro-1-trifluoromethylethyl)-2-methyl-7-nitrobenzo[b]furan | HCID 86753553 | — |
反応手順
Into a mixture of 2-methyl-7-nitrobenzo[b]furan (200 mg) and aluminum chloride (301 mg) in dichloromethane was passed hexafluoroacetone gas which was made from hexafluoroacetone trihydrate (4.7 ml) and conc. sulfuric acid (15 ml). The mixture was stirred at ambient temperature for 4 hours and then, cooled to 4° C. To the mixture was added 1N-hydrochloric acid dropwise. The organic layer was separated, washed with brine, dried over sodium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica gel and the obtained oil was crystallized from n-hexane to give 3-(1-hydroxy-2,2,2-trifluoro-1-trifluoromethylethyl)-2-methyl-7-nitrobenzo[b]furan (265 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05858995 |
| 出典データセット | uspto-grants-1999_01 |
| ORD ID | ord-9ad3bf85b765418e9a85d1c8f96c856a |
| 出典メモ | uspto-grants-1999_01 |